A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11535n54



Internal ID22779430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101325082..101484174hg38UCSC Ensembl
chr7:100968363..101127455hg19UCSC Ensembl
chr7:100755083..100914175hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38159093
hg19159093
hg18159093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607984, nsv607982, nsv607980
SamplesHGDP01065, NINDS_195, 1780854477_A, NINDS_88
Known GenesCOL26A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11535n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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